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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QEV5
Term | Name | Level | Count |
---|---|---|---|
GO:0001932 | regulation of protein phosphorylation | 7 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031399 | regulation of protein modification process | 6 | 2 |
GO:0042325 | regulation of phosphorylation | 7 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1901407 | obsolete regulation of phosphorylation of RNA polymerase II C-terminal domain | 8 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018208 | peptidyl-proline modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0016853 | isomerase activity | 2 | 9 |
GO:0016859 | cis-trans isomerase activity | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.462 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.607 |
CLV_PCSK_FUR_1 | 369 | 373 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 371 | 373 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 681 | 683 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 218 | 224 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 677 | 683 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.569 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.445 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.797 |
DOC_CYCLIN_RxL_1 | 134 | 141 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 11 | 17 | PF00134 | 0.434 |
DOC_MAPK_gen_1 | 218 | 228 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 43 | 51 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 677 | 687 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 221 | 230 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 307 | 314 | PF00069 | 0.686 |
DOC_MAPK_MEF2A_6 | 476 | 485 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 562 | 571 | PF00069 | 0.565 |
DOC_MAPK_RevD_3 | 357 | 372 | PF00069 | 0.587 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.513 |
DOC_PP2B_PxIxI_1 | 480 | 486 | PF00149 | 0.604 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 409 | 416 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 456 | 461 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 614 | 622 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.626 |
LIG_BIR_III_4 | 524 | 528 | PF00653 | 0.546 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.556 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.638 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.605 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.509 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.611 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.468 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.503 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.448 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.558 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.560 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.645 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.447 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.447 |
LIG_Integrin_RGD_1 | 581 | 583 | PF01839 | 0.621 |
LIG_LIR_Apic_2 | 360 | 364 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 100 | 111 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 381 | 391 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 636 | 644 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 610 | 615 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 636 | 640 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 641 | 647 | PF02991 | 0.447 |
LIG_MYND_1 | 16 | 20 | PF01753 | 0.452 |
LIG_NRBOX | 139 | 145 | PF00104 | 0.496 |
LIG_PTB_Apo_2 | 507 | 514 | PF02174 | 0.562 |
LIG_PTB_Phospho_1 | 507 | 513 | PF10480 | 0.658 |
LIG_RPA_C_Fungi | 218 | 230 | PF08784 | 0.486 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.696 |
LIG_SH2_PTP2 | 309 | 312 | PF00017 | 0.588 |
LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.610 |
LIG_SH2_PTP2 | 451 | 454 | PF00017 | 0.496 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.687 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.552 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.485 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.678 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.677 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.601 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.557 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.493 |
LIG_SUMO_SIM_anti_2 | 19 | 29 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 565 | 571 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 181 | 189 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.496 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.510 |
LIG_TYR_ITIM | 630 | 635 | PF00017 | 0.281 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.743 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.549 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.651 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.466 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.561 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.540 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.638 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.630 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.776 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.281 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.621 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.648 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.665 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.484 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.525 |
MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.601 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.600 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.503 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.611 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.685 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.579 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.281 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.639 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.552 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.702 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.500 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.611 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.799 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.671 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.594 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.645 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.525 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.584 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.447 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.392 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.473 |
MOD_N-GLC_2 | 105 | 107 | PF02516 | 0.457 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.605 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.506 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.531 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.448 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.508 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.315 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.410 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.511 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.595 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.530 |
MOD_NEK2_2 | 461 | 466 | PF00069 | 0.563 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.315 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.383 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.621 |
MOD_PKA_1 | 551 | 557 | PF00069 | 0.574 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.644 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.607 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.552 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.351 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.421 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.591 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.561 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.533 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.506 |
MOD_Plk_2-3 | 636 | 642 | PF00069 | 0.297 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.625 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.593 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.513 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.583 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.441 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.624 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.777 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.493 |
MOD_SUMO_rev_2 | 579 | 587 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 617 | 626 | PF00179 | 0.281 |
TRG_DiLeu_BaEn_1 | 565 | 570 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.697 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 46 | 49 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.463 |
TRG_NLS_MonoCore_2 | 220 | 225 | PF00514 | 0.634 |
TRG_NLS_MonoExtN_4 | 218 | 225 | PF00514 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB00 | Leptomonas seymouri | 57% | 100% |
A0A3Q8ICH7 | Leishmania donovani | 87% | 98% |
A0A422MVZ8 | Trypanosoma rangeli | 37% | 100% |
A4H8I6 | Leishmania braziliensis | 78% | 100% |
A4HWW3 | Leishmania infantum | 87% | 98% |
C9ZPQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |