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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFH4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.663 |
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.749 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.385 |
CLV_PCSK_FUR_1 | 271 | 275 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 517 | 519 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.539 |
DOC_CKS1_1 | 401 | 406 | PF01111 | 0.586 |
DOC_CYCLIN_RxL_1 | 412 | 422 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.554 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 449 | PF00134 | 0.640 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.588 |
DOC_MAPK_DCC_7 | 104 | 114 | PF00069 | 0.280 |
DOC_MAPK_DCC_7 | 70 | 78 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 87 | 94 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 22 | 30 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 406 | 413 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 70 | 78 | PF00069 | 0.334 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.514 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.566 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.369 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 297 | 301 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 470 | 479 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 546 | 553 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 554 | 560 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.636 |
LIG_Actin_WH2_2 | 552 | 570 | PF00022 | 0.570 |
LIG_AP2alpha_1 | 63 | 67 | PF02296 | 0.672 |
LIG_AP2alpha_2 | 300 | 302 | PF02296 | 0.612 |
LIG_APCC_ABBA_1 | 248 | 253 | PF00400 | 0.414 |
LIG_BRCT_BRCA1_1 | 595 | 599 | PF00533 | 0.680 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.485 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.501 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.453 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.563 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.569 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.529 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.560 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.560 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.387 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.530 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.531 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.681 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 305 | 313 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 323 | 330 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.503 |
LIG_MLH1_MIPbox_1 | 595 | 599 | PF16413 | 0.525 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.630 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.332 |
LIG_Rb_pABgroove_1 | 245 | 253 | PF01858 | 0.308 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.370 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.496 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 307 | 310 | PF00017 | 0.381 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.562 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.571 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.588 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.463 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.553 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.575 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.613 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.535 |
LIG_SUMO_SIM_anti_2 | 391 | 398 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 434 | 440 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 110 | 116 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 345 | 353 | PF11976 | 0.522 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.455 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.574 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.501 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.758 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.536 |
LIG_TYR_ITSM | 398 | 405 | PF00017 | 0.510 |
MOD_CDC14_SPxK_1 | 515 | 518 | PF00782 | 0.513 |
MOD_CDC14_SPxK_1 | 539 | 542 | PF00782 | 0.509 |
MOD_CDK_SPK_2 | 512 | 517 | PF00069 | 0.782 |
MOD_CDK_SPK_2 | 82 | 87 | PF00069 | 0.433 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.587 |
MOD_CDK_SPxK_1 | 512 | 518 | PF00069 | 0.514 |
MOD_CDK_SPxK_1 | 536 | 542 | PF00069 | 0.615 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.426 |
MOD_CDK_SPxxK_3 | 134 | 141 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 82 | 89 | PF00069 | 0.588 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.485 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.610 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.743 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.714 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.647 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.661 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.763 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.686 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.425 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.554 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.614 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.602 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.619 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.568 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.541 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.722 |
MOD_Cter_Amidation | 288 | 291 | PF01082 | 0.521 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.465 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.517 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.719 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.647 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.481 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.742 |
MOD_GlcNHglycan | 358 | 362 | PF01048 | 0.630 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.746 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.674 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.611 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.789 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.790 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.473 |
MOD_GlcNHglycan | 98 | 102 | PF01048 | 0.491 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.485 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.690 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.682 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.607 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.540 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.448 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.704 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.593 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.678 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.371 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.559 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.639 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.619 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.649 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.577 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.628 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.399 |
MOD_PK_1 | 487 | 493 | PF00069 | 0.508 |
MOD_PKA_1 | 487 | 493 | PF00069 | 0.508 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.554 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.697 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.705 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.605 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.478 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.735 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.651 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.656 |
MOD_PKB_1 | 518 | 526 | PF00069 | 0.685 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.562 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.467 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.520 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.689 |
MOD_Plk_2-3 | 154 | 160 | PF00069 | 0.378 |
MOD_Plk_2-3 | 530 | 536 | PF00069 | 0.652 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.577 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.514 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.563 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.600 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.413 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.532 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.592 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.423 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.614 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.532 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.578 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.587 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.709 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.747 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.349 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.555 |
MOD_SUMO_rev_2 | 252 | 256 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.588 |
TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.346 |
TRG_DiLeu_LyEn_5 | 165 | 170 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I592 | Leptomonas seymouri | 52% | 97% |
A0A1X0P512 | Trypanosomatidae | 35% | 100% |
A0A3S7X0H0 | Leishmania donovani | 74% | 100% |
A0A422NTD4 | Trypanosoma rangeli | 32% | 100% |
A4I2N4 | Leishmania infantum | 74% | 100% |
D0A5Q0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AD25 | Leishmania major | 74% | 100% |
E9AYV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
V5BSP9 | Trypanosoma cruzi | 33% | 100% |