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:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9ASZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000049 | tRNA binding | 5 | 3 |
GO:0008173 | RNA methyltransferase activity | 4 | 3 |
GO:0008175 | tRNA methyltransferase activity | 5 | 3 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 3 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 3 |
GO:0016428 | tRNA (cytosine-5-)-methyltransferase activity | 7 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 3 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.254 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.679 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.258 |
CLV_Separin_Metazoa | 302 | 306 | PF03568 | 0.471 |
DEG_APCC_DBOX_1 | 392 | 400 | PF00400 | 0.458 |
DEG_APCC_DBOX_1 | 690 | 698 | PF00400 | 0.378 |
DEG_SCF_FBW7_1 | 103 | 110 | PF00400 | 0.518 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.596 |
DOC_CKS1_1 | 104 | 109 | PF01111 | 0.520 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.652 |
DOC_CKS1_1 | 432 | 437 | PF01111 | 0.451 |
DOC_CYCLIN_RxL_1 | 260 | 272 | PF00134 | 0.346 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.451 |
DOC_MAPK_gen_1 | 253 | 259 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 263 | 269 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 654 | 664 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 691 | 699 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 722 | 731 | PF00069 | 0.356 |
DOC_MAPK_HePTP_8 | 652 | 664 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 212 | 220 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 655 | 664 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 722 | 731 | PF00069 | 0.398 |
DOC_MAPK_NFAT4_5 | 724 | 732 | PF00069 | 0.386 |
DOC_MIT_MIM_1 | 687 | 697 | PF04212 | 0.533 |
DOC_PP1_RVXF_1 | 264 | 270 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 626 | 633 | PF00149 | 0.460 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.451 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.379 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.531 |
DOC_PP4_MxPP_1 | 188 | 191 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.690 |
DOC_USP7_MATH_2 | 236 | 242 | PF00917 | 0.390 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.685 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.624 |
DOC_USP7_UBL2_3 | 513 | 517 | PF12436 | 0.738 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 359 | 369 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 640 | 649 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 654 | 662 | PF00244 | 0.351 |
LIG_Actin_WH2_2 | 306 | 324 | PF00022 | 0.482 |
LIG_Actin_WH2_2 | 339 | 357 | PF00022 | 0.484 |
LIG_BIR_III_2 | 231 | 235 | PF00653 | 0.584 |
LIG_BIR_III_4 | 412 | 416 | PF00653 | 0.531 |
LIG_Clathr_ClatBox_1 | 703 | 707 | PF01394 | 0.348 |
LIG_CSL_BTD_1 | 330 | 333 | PF09270 | 0.451 |
LIG_eIF4E_1 | 239 | 245 | PF01652 | 0.304 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.399 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.346 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.507 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.495 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.430 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.596 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.451 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.531 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.742 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.608 |
LIG_LIR_Apic_2 | 102 | 107 | PF02991 | 0.402 |
LIG_LIR_Apic_2 | 571 | 576 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 571 | 575 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 636 | 642 | PF02991 | 0.307 |
LIG_MAD2 | 60 | 68 | PF02301 | 0.495 |
LIG_PCNA_PIPBox_1 | 164 | 173 | PF02747 | 0.428 |
LIG_PCNA_PIPBox_1 | 566 | 575 | PF02747 | 0.491 |
LIG_PDZ_Class_3 | 757 | 762 | PF00595 | 0.753 |
LIG_PTB_Apo_2 | 42 | 49 | PF02174 | 0.535 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.522 |
LIG_SH2_GRB2like | 51 | 54 | PF00017 | 0.250 |
LIG_SH2_NCK_1 | 438 | 442 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 573 | 577 | PF00017 | 0.433 |
LIG_SH2_SRC | 573 | 576 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 717 | 721 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.465 |
LIG_SH3_1 | 573 | 579 | PF00018 | 0.427 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.645 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.502 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.484 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.359 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.399 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.471 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.565 |
LIG_SUMO_SIM_anti_2 | 617 | 624 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 617 | 624 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 702 | 707 | PF11976 | 0.373 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.349 |
LIG_UBA3_1 | 216 | 224 | PF00899 | 0.378 |
LIG_UBA3_1 | 327 | 334 | PF00899 | 0.522 |
LIG_UBA3_1 | 703 | 710 | PF00899 | 0.490 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.529 |
MOD_CDK_SPK_2 | 329 | 334 | PF00069 | 0.451 |
MOD_CDK_SPxxK_3 | 205 | 212 | PF00069 | 0.363 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.297 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.693 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.359 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.503 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.450 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.370 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.735 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.382 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.343 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.451 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.742 |
MOD_CK2_1 | 689 | 695 | PF00069 | 0.388 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.672 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.262 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.322 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.678 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.417 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.380 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.630 |
MOD_GlcNHglycan | 87 | 91 | PF01048 | 0.461 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.518 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.396 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.671 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.386 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.451 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.604 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.769 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.593 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.501 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.663 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.377 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.447 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.320 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.481 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.555 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.475 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.397 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.487 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.352 |
MOD_NEK2_1 | 716 | 721 | PF00069 | 0.203 |
MOD_NEK2_2 | 317 | 322 | PF00069 | 0.463 |
MOD_PIKK_1 | 685 | 691 | PF00454 | 0.454 |
MOD_PKA_1 | 516 | 522 | PF00069 | 0.621 |
MOD_PKA_1 | 654 | 660 | PF00069 | 0.515 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.731 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.474 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.315 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.353 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.499 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.555 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.403 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.342 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.686 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.359 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.414 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.447 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.519 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.365 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.503 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.658 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.451 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.451 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.619 |
MOD_SUMO_for_1 | 512 | 515 | PF00179 | 0.748 |
MOD_SUMO_rev_2 | 249 | 255 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 481 | 490 | PF00179 | 0.650 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 690 | 693 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 721 | 724 | PF00400 | 0.350 |
TRG_NLS_Bipartite_1 | 253 | 267 | PF00514 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 567 | 571 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZE7 | Leptomonas seymouri | 77% | 98% |
A0A1X0P7M3 | Trypanosomatidae | 59% | 100% |
A0A3Q8IJ07 | Leishmania donovani | 32% | 100% |
A0A3Q8INR5 | Leishmania donovani | 92% | 99% |
A0A3R7M922 | Trypanosoma rangeli | 29% | 95% |
A0A3R7NNX1 | Trypanosoma rangeli | 57% | 100% |
A4HP86 | Leishmania braziliensis | 85% | 100% |
A4IDJ1 | Leishmania infantum | 92% | 99% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AHJ5 | Leishmania infantum | 33% | 100% |
O13935 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P38205 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q08J23 | Homo sapiens | 31% | 99% |
Q1HFZ0 | Mus musculus | 31% | 100% |
Q28E61 | Xenopus tropicalis | 32% | 95% |
Q4Q1K4 | Leishmania major | 91% | 100% |
Q4V7N2 | Xenopus laevis | 34% | 100% |
Q5ZLV4 | Gallus gallus | 32% | 96% |
Q9HGQ2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
V5DCJ5 | Trypanosoma cruzi | 63% | 100% |