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: E9AJR7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 487 | 493 | PF00089 | 0.449 |
CLV_MEL_PAP_1 | 71 | 77 | PF00089 | 0.357 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.784 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 269 | 277 | PF00400 | 0.545 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.621 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.437 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.738 |
DEG_SPOP_SBC_1 | 104 | 108 | PF00917 | 0.681 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.489 |
DOC_CYCLIN_RxL_1 | 289 | 299 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.509 |
DOC_MAPK_DCC_7 | 546 | 555 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 167 | 176 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 546 | 555 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.468 |
DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.480 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.677 |
DOC_PP4_FxxP_1 | 404 | 407 | PF00568 | 0.287 |
DOC_PP4_FxxP_1 | 522 | 525 | PF00568 | 0.516 |
DOC_PP4_FxxP_1 | 596 | 599 | PF00568 | 0.624 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 238 | 245 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 367 | 376 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 417 | 427 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 490 | 497 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 546 | 550 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 570 | 578 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.592 |
LIG_AP2alpha_2 | 581 | 583 | PF02296 | 0.678 |
LIG_APCC_ABBA_1 | 294 | 299 | PF00400 | 0.567 |
LIG_APCC_ABBA_1 | 87 | 92 | PF00400 | 0.521 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.630 |
LIG_deltaCOP1_diTrp_1 | 184 | 194 | PF00928 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 610 | 619 | PF00928 | 0.599 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.268 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.439 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.413 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.462 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.461 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.732 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.740 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.542 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.574 |
LIG_LIR_Apic_2 | 380 | 385 | PF02991 | 0.650 |
LIG_LIR_Apic_2 | 520 | 525 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 595 | 599 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 616 | 626 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.531 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.729 |
LIG_NRBOX | 448 | 454 | PF00104 | 0.407 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.399 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.530 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.611 |
LIG_SH2_STAT3 | 83 | 86 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.413 |
LIG_SH3_1 | 250 | 256 | PF00018 | 0.524 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.464 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.760 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.473 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.689 |
LIG_SUMO_SIM_par_1 | 292 | 299 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 525 | 531 | PF11976 | 0.469 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.635 |
MOD_CDK_SPK_2 | 541 | 546 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 323 | 330 | PF00069 | 0.556 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.612 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.446 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.740 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.653 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.778 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.551 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.462 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.548 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.533 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.647 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.573 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.712 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.792 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.548 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.669 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.685 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.717 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.691 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.589 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.697 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.741 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.647 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.483 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.336 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.651 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.663 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.725 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.614 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.472 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.787 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.405 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.479 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.626 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.671 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.590 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.441 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.533 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.577 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.472 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.561 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.598 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.433 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.608 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.479 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.682 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.539 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.484 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.427 |
MOD_PKA_1 | 223 | 229 | PF00069 | 0.765 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.595 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.744 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.767 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.519 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.521 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.451 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.510 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.622 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.374 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.487 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.681 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.618 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.449 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.608 |
MOD_Plk_1 | 624 | 630 | PF00069 | 0.606 |
MOD_Plk_2-3 | 198 | 204 | PF00069 | 0.601 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.729 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.610 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.399 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.710 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.757 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.610 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.698 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.690 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.466 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.516 |
MOD_SUMO_rev_2 | 166 | 174 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_4 | 328 | 334 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 302 | 307 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 437 | 442 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 522 | 527 | PF01217 | 0.496 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.590 |
TRG_NES_CRM1_1 | 163 | 175 | PF08389 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 177 | 182 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 193 | 198 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I3 | Leptomonas seymouri | 56% | 88% |
A0A1X0P8P7 | Trypanosomatidae | 43% | 100% |
A0A3R7NU48 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H535 | Leishmania donovani | 88% | 100% |
A4H3K3 | Leishmania braziliensis | 76% | 100% |
A4HRU3 | Leishmania infantum | 88% | 100% |
D0A241 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACH8 | Leishmania major | 86% | 100% |
V5BSU9 | Trypanosoma cruzi | 42% | 100% |