Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HEJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016553 | base conversion or substitution editing | 6 | 1 |
GO:0016554 | cytidine to uridine editing | 7 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.227 |
CLV_PCSK_PC7_1 | 216 | 222 | PF00082 | 0.363 |
CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.327 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.553 |
DEG_SPOP_SBC_1 | 673 | 677 | PF00917 | 0.322 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.227 |
DOC_CYCLIN_yCln2_LP_2 | 633 | 639 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 220 | 227 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 36 | 44 | PF00069 | 0.430 |
DOC_MAPK_RevD_3 | 206 | 221 | PF00069 | 0.363 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 436 | 439 | PF00568 | 0.227 |
DOC_PP4_FxxP_1 | 529 | 532 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.438 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.399 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.216 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 534 | 538 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 699 | 704 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.296 |
LIG_Actin_RPEL_3 | 259 | 278 | PF02755 | 0.227 |
LIG_Actin_WH2_2 | 651 | 669 | PF00022 | 0.463 |
LIG_AP2alpha_2 | 93 | 95 | PF02296 | 0.335 |
LIG_APCC_ABBA_1 | 231 | 236 | PF00400 | 0.466 |
LIG_APCC_ABBAyCdc20_2 | 535 | 541 | PF00400 | 0.536 |
LIG_BIR_III_4 | 401 | 405 | PF00653 | 0.335 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.827 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.335 |
LIG_EH1_1 | 456 | 464 | PF00400 | 0.374 |
LIG_EH1_1 | 465 | 473 | PF00400 | 0.335 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.249 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.227 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.378 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.408 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.399 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.480 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.335 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.378 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.557 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 296 | 300 | PF02991 | 0.341 |
LIG_LIR_Apic_2 | 306 | 310 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 526 | 532 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 198 | 208 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 57 | 65 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 653 | 660 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.361 |
LIG_PCNA_yPIPBox_3 | 447 | 456 | PF02747 | 0.432 |
LIG_Pex14_1 | 201 | 205 | PF04695 | 0.480 |
LIG_PTB_Apo_2 | 384 | 391 | PF02174 | 0.335 |
LIG_PTB_Phospho_1 | 384 | 390 | PF10480 | 0.480 |
LIG_Rb_pABgroove_1 | 603 | 611 | PF01858 | 0.379 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.227 |
LIG_SH2_CRK | 59 | 63 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 609 | 612 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.355 |
LIG_SH2_SRC | 609 | 612 | PF00017 | 0.299 |
LIG_SH2_SRC | 679 | 682 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.403 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.319 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.390 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.335 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.355 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.651 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.479 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.319 |
LIG_Sin3_3 | 111 | 118 | PF02671 | 0.266 |
LIG_SUMO_SIM_anti_2 | 469 | 475 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 485 | 491 | PF11976 | 0.335 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.656 |
LIG_TRFH_1 | 529 | 533 | PF08558 | 0.531 |
LIG_WRC_WIRS_1 | 294 | 299 | PF05994 | 0.227 |
LIG_WRC_WIRS_1 | 47 | 52 | PF05994 | 0.447 |
LIG_WW_2 | 40 | 43 | PF00397 | 0.645 |
LIG_WW_3 | 531 | 535 | PF00397 | 0.559 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.850 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.427 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.347 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.305 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.351 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.470 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.490 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.495 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.721 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.404 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.335 |
MOD_Cter_Amidation | 218 | 221 | PF01082 | 0.335 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.391 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.483 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.353 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.808 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.761 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.403 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.335 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.335 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.331 |
MOD_GlcNHglycan | 426 | 432 | PF01048 | 0.461 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.342 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.664 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.550 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.648 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.404 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.537 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.553 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.406 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.377 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.396 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.450 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.480 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.726 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.350 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.422 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.252 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.331 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.552 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.340 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.493 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.480 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.420 |
MOD_N-GLC_1 | 584 | 589 | PF02516 | 0.556 |
MOD_N-GLC_1 | 610 | 615 | PF02516 | 0.314 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.391 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.335 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.447 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.615 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.524 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.363 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.480 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.335 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.349 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.335 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.484 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.689 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.480 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.265 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.335 |
MOD_PKA_1 | 287 | 293 | PF00069 | 0.227 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.698 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.329 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.237 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.756 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.385 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.301 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.535 |
MOD_PKB_1 | 264 | 272 | PF00069 | 0.227 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.447 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.420 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.423 |
MOD_Plk_2-3 | 20 | 26 | PF00069 | 0.580 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.346 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.312 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.419 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.412 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.523 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.303 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.425 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.249 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.334 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.335 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.399 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.490 |
TRG_NES_CRM1_1 | 597 | 610 | PF08389 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.393 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT36 | Leptomonas seymouri | 63% | 96% |
A0A1X0NYA6 | Trypanosomatidae | 52% | 100% |
A0A3R7MPK5 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WZ63 | Leishmania donovani | 84% | 95% |
A4I1K0 | Leishmania infantum | 84% | 95% |
C9ZK34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AXN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 95% |
Q4Q9T7 | Leishmania major | 85% | 100% |
V5BHU4 | Trypanosoma cruzi | 50% | 100% |