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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q8I7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.777 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.542 |
CLV_PCSK_FUR_1 | 275 | 279 | PF00082 | 0.678 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.635 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.827 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.598 |
CLV_Separin_Metazoa | 342 | 346 | PF03568 | 0.736 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.456 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.573 |
DEG_SCF_FBW7_2 | 217 | 224 | PF00400 | 0.688 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.783 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.664 |
DOC_MAPK_gen_1 | 486 | 494 | PF00069 | 0.523 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.583 |
DOC_PP4_FxxP_1 | 340 | 343 | PF00568 | 0.558 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.741 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.776 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 409 | 415 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 451 | 458 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 135 | 153 | PF00022 | 0.531 |
LIG_BIR_III_2 | 42 | 46 | PF00653 | 0.714 |
LIG_BIR_III_4 | 426 | 430 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.635 |
LIG_deltaCOP1_diTrp_1 | 326 | 332 | PF00928 | 0.525 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.775 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.649 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.501 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.481 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.792 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.536 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.643 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.766 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.701 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.593 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.553 |
LIG_GBD_Chelix_1 | 142 | 150 | PF00786 | 0.471 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 338 | 343 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.728 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.495 |
LIG_Pex14_1 | 327 | 331 | PF04695 | 0.524 |
LIG_RPA_C_Fungi | 153 | 165 | PF08784 | 0.573 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.773 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.742 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.542 |
LIG_SH3_1 | 101 | 107 | PF00018 | 0.581 |
LIG_SH3_2 | 104 | 109 | PF14604 | 0.690 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.581 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.771 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.531 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.794 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.637 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.664 |
LIG_WW_3 | 342 | 346 | PF00397 | 0.736 |
MOD_CDK_SPK_2 | 81 | 86 | PF00069 | 0.674 |
MOD_CDK_SPxxK_3 | 81 | 88 | PF00069 | 0.668 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.712 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.665 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.695 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.703 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.663 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.773 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.683 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.655 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.572 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.711 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.671 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.633 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.778 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.712 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.681 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.532 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.562 |
MOD_Cter_Amidation | 124 | 127 | PF01082 | 0.470 |
MOD_Cter_Amidation | 383 | 386 | PF01082 | 0.700 |
MOD_DYRK1A_RPxSP_1 | 204 | 208 | PF00069 | 0.645 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.601 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.776 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.562 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.672 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.592 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.745 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.701 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.669 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.616 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.687 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.722 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.515 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.584 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.749 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.676 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.503 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.544 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.536 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.339 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.628 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.657 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.708 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.597 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.775 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.677 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.705 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.789 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.545 |
MOD_PKA_1 | 385 | 391 | PF00069 | 0.784 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.704 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.607 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.575 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.693 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.661 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.704 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.575 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.406 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.567 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.532 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.749 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.538 |
MOD_PKB_1 | 74 | 82 | PF00069 | 0.703 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.545 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.576 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.525 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.572 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.627 |
MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.773 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.606 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.717 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.527 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.747 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.789 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.566 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.662 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.792 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.644 |
TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.616 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.703 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8G0 | Leptomonas seymouri | 63% | 100% |
A0A0S4IT28 | Bodo saltans | 36% | 100% |
A0A1X0NYF9 | Trypanosomatidae | 47% | 100% |
A0A3Q8IDQ0 | Leishmania donovani | 95% | 100% |
A0A3R7M5S0 | Trypanosoma rangeli | 46% | 100% |
A4HGC4 | Leishmania braziliensis | 79% | 100% |
A4I3F7 | Leishmania infantum | 95% | 100% |
D0A7Y3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AZP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BKT5 | Trypanosoma cruzi | 45% | 100% |