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: 6 |
Silverman et al. | no | yes: 3 |
Pissara et al. | no | yes: 12 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AP92
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004177 | aminopeptidase activity | 5 | 6 |
GO:0008233 | peptidase activity | 3 | 6 |
GO:0008238 | exopeptidase activity | 4 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 477 | 483 | PF00089 | 0.326 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.721 |
CLV_PCSK_FUR_1 | 18 | 22 | PF00082 | 0.474 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.342 |
CLV_PCSK_FUR_1 | 76 | 80 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.216 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 490 | 492 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 554 | 556 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.721 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.558 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.519 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.285 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.602 |
DEG_SCF_FBW7_1 | 499 | 506 | PF00400 | 0.322 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.472 |
DOC_ANK_TNKS_1 | 349 | 356 | PF00023 | 0.304 |
DOC_CKS1_1 | 500 | 505 | PF01111 | 0.490 |
DOC_CYCLIN_RxL_1 | 190 | 199 | PF00134 | 0.379 |
DOC_CYCLIN_yCln2_LP_2 | 527 | 533 | PF00134 | 0.388 |
DOC_MAPK_FxFP_2 | 436 | 439 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 450 | 457 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 238 | 247 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.389 |
DOC_PP4_FxxP_1 | 436 | 439 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.175 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.665 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 21 | 26 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 282 | 291 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 362 | 369 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 397 | 407 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.556 |
LIG_Actin_WH2_2 | 302 | 318 | PF00022 | 0.417 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.623 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.464 |
LIG_DLG_GKlike_1 | 23 | 30 | PF00625 | 0.468 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.302 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.315 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.331 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.357 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.480 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.370 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.388 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.463 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.457 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.355 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.494 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.564 |
LIG_GSK3_LRP6_1 | 499 | 504 | PF00069 | 0.316 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 532 | 540 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.440 |
LIG_MAD2 | 73 | 81 | PF02301 | 0.572 |
LIG_PCNA_yPIPBox_3 | 209 | 223 | PF02747 | 0.340 |
LIG_PCNA_yPIPBox_3 | 316 | 328 | PF02747 | 0.353 |
LIG_Pex14_2 | 436 | 440 | PF04695 | 0.449 |
LIG_RPA_C_Fungi | 18 | 30 | PF08784 | 0.586 |
LIG_SH2_STAT3 | 335 | 338 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.440 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.413 |
LIG_SUMO_SIM_anti_2 | 522 | 528 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.352 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.402 |
MOD_CDC14_SPxK_1 | 227 | 230 | PF00782 | 0.417 |
MOD_CDK_SPK_2 | 108 | 113 | PF00069 | 0.448 |
MOD_CDK_SPxK_1 | 224 | 230 | PF00069 | 0.417 |
MOD_CDK_SPxxK_3 | 547 | 554 | PF00069 | 0.671 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.466 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.309 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.354 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.422 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.543 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.672 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.754 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.676 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.573 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.266 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.395 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.454 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.394 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.440 |
MOD_Cter_Amidation | 203 | 206 | PF01082 | 0.363 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.389 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.535 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.511 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.516 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.226 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.329 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.290 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.398 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.339 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.560 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.653 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.769 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.667 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.667 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.589 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.470 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.175 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.436 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.311 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.321 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.345 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.530 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.394 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.621 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.731 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.533 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.679 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.637 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.511 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.285 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.285 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.540 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.499 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.500 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.344 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.595 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.702 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.266 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.425 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.363 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.482 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.475 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.445 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.447 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.316 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.336 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.595 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.451 |
MOD_PKB_1 | 282 | 290 | PF00069 | 0.233 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.528 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.285 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.420 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.425 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.348 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.355 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.561 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.548 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.387 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.502 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.517 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.669 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 555 | 558 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.719 |
TRG_NLS_MonoExtC_3 | 553 | 559 | PF00514 | 0.628 |
TRG_NLS_MonoExtN_4 | 18 | 24 | PF00514 | 0.464 |
TRG_NLS_MonoExtN_4 | 551 | 558 | PF00514 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIM1 | Leptomonas seymouri | 28% | 100% |
A0A0N1IM06 | Leptomonas seymouri | 68% | 98% |
A0A0S4J160 | Bodo saltans | 30% | 100% |
A0A1X0NPS8 | Trypanosomatidae | 46% | 100% |
A0A3Q8IBA7 | Leishmania donovani | 29% | 100% |
A0A3Q8IBP5 | Leishmania donovani | 89% | 98% |
A0A3R7KN75 | Trypanosoma rangeli | 45% | 100% |
A4H757 | Leishmania braziliensis | 80% | 100% |
A4H9X3 | Leishmania braziliensis | 30% | 100% |
A4HVJ6 | Leishmania infantum | 89% | 98% |
D0A6Q9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AGR8 | Leishmania infantum | 29% | 100% |
E9ARW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4QDK5 | Leishmania major | 30% | 100% |
Q4QG86 | Leishmania major | 85% | 99% |
V5BFG1 | Trypanosoma cruzi | 47% | 100% |