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: 20 |
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: 2, no: 13 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: Q4QD31
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.368 |
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.374 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.579 |
CLV_PCSK_PC7_1 | 384 | 390 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.562 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.510 |
DEG_SCF_FBW7_1 | 201 | 207 | PF00400 | 0.408 |
DOC_ANK_TNKS_1 | 216 | 223 | PF00023 | 0.274 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.407 |
DOC_PP1_RVXF_1 | 152 | 158 | PF00149 | 0.274 |
DOC_PP1_RVXF_1 | 230 | 236 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.687 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.639 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.585 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.628 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.571 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.488 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.465 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.401 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.381 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.501 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.407 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.396 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.364 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.636 |
LIG_Integrin_RGD_1 | 71 | 73 | PF01839 | 0.368 |
LIG_LIR_Apic_2 | 411 | 415 | PF02991 | 0.603 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 182 | 192 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.485 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.355 |
LIG_Pex14_2 | 408 | 412 | PF04695 | 0.480 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.431 |
LIG_REV1ctd_RIR_1 | 165 | 174 | PF16727 | 0.394 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.556 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.380 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.463 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.589 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.346 |
LIG_TYR_ITSM | 90 | 97 | PF00017 | 0.508 |
LIG_WRC_WIRS_1 | 409 | 414 | PF05994 | 0.508 |
MOD_CDK_SPxK_1 | 438 | 444 | PF00069 | 0.576 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.591 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.353 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.644 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.502 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.593 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.497 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.768 |
MOD_GlcNHglycan | 394 | 399 | PF01048 | 0.527 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.460 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.582 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.380 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.582 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.704 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.432 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.524 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.462 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.510 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.472 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.378 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.538 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.605 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.601 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.401 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.203 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.594 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.561 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.497 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.497 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.434 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.467 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.416 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.466 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.291 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.412 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.666 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.404 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.594 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.578 |
TRG_DiLeu_BaEn_4 | 64 | 70 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.590 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S2 | Leptomonas seymouri | 77% | 100% |
A0A0S4JFV2 | Bodo saltans | 50% | 100% |
A0A1X0NX05 | Trypanosomatidae | 59% | 100% |
A0A3S7WVR3 | Leishmania donovani | 96% | 100% |
A0A3S7X3U7 | Leishmania donovani | 30% | 100% |
A0A422N7V9 | Trypanosoma rangeli | 58% | 100% |
A4HBI1 | Leishmania braziliensis | 87% | 100% |
A4HIR9 | Leishmania braziliensis | 31% | 100% |
A4HYK3 | Leishmania infantum | 96% | 100% |
A4I615 | Leishmania infantum | 30% | 100% |
C9ZHV2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AUF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q6V8 | Leishmania major | 31% | 100% |
V5C0D1 | Trypanosoma cruzi | 58% | 100% |