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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0031985 | Golgi cisterna | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: E9AV97
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 8 |
GO:0007030 | Golgi organization | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016043 | cellular component organization | 3 | 8 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
GO:0000301 | retrograde transport, vesicle recycling within Golgi | 7 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.701 |
CLV_C14_Caspase3-7 | 566 | 570 | PF00656 | 0.614 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 375 | 381 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.300 |
CLV_Separin_Metazoa | 387 | 391 | PF03568 | 0.634 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.643 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.627 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.623 |
DEG_SCF_FBW7_1 | 531 | 537 | PF00400 | 0.603 |
DEG_SPOP_SBC_1 | 45 | 49 | PF00917 | 0.618 |
DOC_CKS1_1 | 531 | 536 | PF01111 | 0.605 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 433 | 442 | PF00134 | 0.606 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 541 | 550 | PF00069 | 0.678 |
DOC_MAPK_MEF2A_6 | 344 | 352 | PF00069 | 0.623 |
DOC_MIT_MIM_1 | 303 | 311 | PF04212 | 0.630 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.704 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.789 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.643 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.808 |
LIG_14-3-3_CanoR_1 | 154 | 164 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 379 | 389 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 38 | 45 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 503 | 512 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 577 | 586 | PF00244 | 0.715 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.534 |
LIG_AP2alpha_2 | 162 | 164 | PF02296 | 0.627 |
LIG_APCC_ABBA_1 | 257 | 262 | PF00400 | 0.623 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.718 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.755 |
LIG_CaM_IQ_9 | 336 | 351 | PF13499 | 0.643 |
LIG_EVH1_1 | 490 | 494 | PF00568 | 0.706 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.681 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.768 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.667 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.357 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.749 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.612 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.731 |
LIG_GBD_Chelix_1 | 601 | 609 | PF00786 | 0.313 |
LIG_LIR_Apic_2 | 487 | 493 | PF02991 | 0.714 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 521 | 526 | PF02991 | 0.602 |
LIG_MYND_1 | 57 | 61 | PF01753 | 0.709 |
LIG_SH2_PTP2 | 593 | 596 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.292 |
LIG_SH3_2 | 58 | 63 | PF14604 | 0.715 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.771 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.705 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.601 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.479 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.513 |
LIG_SH3_4 | 290 | 297 | PF00018 | 0.578 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.707 |
LIG_SUMO_SIM_par_1 | 607 | 614 | PF11976 | 0.518 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.592 |
LIG_TRAF2_2 | 291 | 296 | PF00917 | 0.696 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.674 |
LIG_WRC_WIRS_1 | 568 | 573 | PF05994 | 0.492 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.657 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.689 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.624 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.656 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.683 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.601 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.551 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.574 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.659 |
MOD_Cter_Amidation | 142 | 145 | PF01082 | 0.510 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.618 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.721 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.574 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.613 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.675 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.681 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.723 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.651 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.665 |
MOD_GlcNHglycan | 535 | 539 | PF01048 | 0.772 |
MOD_GlcNHglycan | 612 | 616 | PF01048 | 0.585 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.668 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.545 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.584 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.589 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.656 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.623 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.578 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.543 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.652 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.544 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.539 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.647 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.649 |
MOD_N-GLC_2 | 484 | 486 | PF02516 | 0.533 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.651 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.621 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.576 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.514 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.609 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.557 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.659 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.650 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.514 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.507 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.530 |
MOD_PKA_1 | 390 | 396 | PF00069 | 0.667 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.612 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.674 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.569 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.584 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.745 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.545 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.604 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.581 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.534 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.653 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.516 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.693 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.783 |
MOD_SUMO_rev_2 | 10 | 16 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 269 | 278 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 286 | 291 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 448 | 454 | PF00179 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 379 | 384 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 419 | 423 | PF00026 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 577 | 581 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCL5 | Leptomonas seymouri | 40% | 94% |
A0A1X0NXW6 | Trypanosomatidae | 23% | 100% |
A0A3Q8IB66 | Leishmania donovani | 89% | 100% |
A4HBX1 | Leishmania braziliensis | 73% | 100% |
A4HZ89 | Leishmania infantum | 88% | 100% |
Q4QC83 | Leishmania major | 88% | 100% |